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FAM58A gene

Known as: FAM58A, MGC29729, FLJ21610 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2008-2016
01220082016

Related topics

Related topics

1 relation
GAREM1 gene

Related mentions per year

Related mentions per year

2008-2017
20002005201020152020
FAM58A gene
GAREM1 gene

Papers overview

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2017
2017
Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotype.
STAR syndrome is a rare X-linked dominant disorder characterized by toe Syndactyly, Telecanthus, Anogenital malformations, and… (More)
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2017
2017
STAR syndrome plus: The first description of a female patient with the lethal form.
The STAR syndrome is a rare X-linked dominant developmental disorder caused by point mutations in the single FAM58A gene or… (More)
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Review
2017
Review
2017
The awakening of the CDK10/Cyclin M protein kinase
Cyclin-dependent kinases (CDKs) play important roles in the control of fundamental cellular processes. Some of the most… (More)
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Review
2016
Review
2016
Ocular manifestations of X-linked dominant FAM58A mutation in toe syndactyly, telecanthus, anogenital, and renal malformations ('STAR') syndrome.
PURPOSE To report the newest ophthalmic manifestations of a mother-daughter pair diagnosed with toe syndactyly, telecanthus… (More)
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2016
2016
STAR syndrome-associated CDK10/Cyclin M regulates actin network architecture and ciliogenesis.
CDK10/CycM is a protein kinase deficient in STAR (toe Syndactyly, Telecanthus and Anogenital and Renal malformations) syndrome… (More)
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2013
2013
CDK10/cyclin M is a protein kinase that controls ETS2 degradation and is deficient in STAR syndrome.
Cyclin-dependent kinases (CDKs) regulate a variety of fundamental cellular processes. CDK10 stands out as one of the last orphan… (More)
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2008
2008
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations
We identified four girls with a consistent constellation of facial dysmorphism and malformations previously reported in a single… (More)
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